"0093-7272-56" National Drug Code (NDC)

NDC Code	0093-7272-56
Package Description	30 TABLET in 1 BOTTLE (0093-7272-56)
Product NDC	0093-7272
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Pioglitazone
Non-Proprietary Name	Pioglitazone
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20150204
Marketing Category Name	ANDA
Application Number	ANDA077210
Manufacturer	Teva Pharmaceuticals USA, Inc.
Substance Name	PIOGLITAZONE HYDROCHLORIDE
Strength	30
Strength Unit	mg/1
Pharmacy Classes	Peroxisome Proliferator Receptor alpha Agonist [EPC], Peroxisome Proliferator Receptor gamma Agonist [EPC], Peroxisome Proliferator-activated Receptor alpha Agonists [MoA], Peroxisome Proliferator-activated Receptor gamma Agonists [MoA], Thiazolidinedione [EPC], Thiazolidinediones [CS]